(Q41930221)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

title

Involvement of the kinesin family members KIF4A and KIF5C in intellectual disability and synaptic function (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

disability affecting intellectual abilities

17 March 2020

main subject

disability

0 references

intellectual disability

1 reference

based on heuristic

inferred from title

1 reference

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

Stefan Haas

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

Lisenka Vissers

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

Hans van Bokhoven

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

Nael Nadif Kasri

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

4

Arjan P M de Brouwer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

12

Tjitske Kleefstra

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

Marjolein H Willemsen

1

object named as

Marjolein H Willemsen

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

Willemijn M Wissink-Lindhout

17 March 2020

3

object named as

Willemijn M Wissink-Lindhout

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

author name string

Wei Ba

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

Melanie Bienek

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

Hao Hu

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

language of work or name

English

0 references

publication date

8 May 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

Journal of Medical Genetics

17 March 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

volume

51

1 reference

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17 March 2020

issue

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

17 March 2020

page(s)

487-494

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:24812067%20AND%20SRC:MED&resulttype=core&format=json

All kinesin superfamily protein, KIF, genes in mouse and human

17 March 2020

cites work

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Kinesin motors and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

A standardized kinesin nomenclature

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Molecular motors in neurons: transport mechanisms and roles in brain function, development, and disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Kinesin superfamily protein 2A (KIF2A) functions in suppression of collateral branch extension.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Defect in synaptic vesicle precursor transport and neuronal cell death in KIF1A motor protein-deficient mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Situs inversus and embryonic ciliary morphogenesis defects in mouse mutants lacking the KIF3A subunit of kinesin-II

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Randomization of left-right asymmetry due to loss of nodal cilia generating leftward flow of extraembryonic fluid in mice lacking KIF3B motor protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

KIF4 motor regulates activity-dependent neuronal survival by suppressing PARP-1 enzymatic activity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Targeted disruption of mouse conventional kinesin heavy chain, kif5B, results in abnormal perinuclear clustering of mitochondria

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Abnormal neurofilament transport caused by targeted disruption of neuronal kinesin heavy chain KIF5A.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Overexpression of motor protein KIF17 enhances spatial and working memory in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Molecular motor KIF5A is essential for GABA(A) receptor transport, and KIF5A deletion causes epilepsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Exome sequencing and disease-network analysis of a single family implicate a mutation in KIF1A in hereditary spastic paraparesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

A kinesin heavy chain (KIF5A) mutation in hereditary spastic paraplegia (SPG10)

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

KIF7 mutations cause fetal hydrolethalus and acrocallosal syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Mutations in KIF7 link Joubert syndrome with Sonic Hedgehog signaling and microtubule dynamics

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Deep sequencing reveals 50 novel genes for recessive cognitive disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Heterozygous mutations of the kinesin KIF21A in congenital fibrosis of the extraocular muscles type 1 (CFEOM1).

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Diagnostic exome sequencing in persons with severe intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Rapid synthesis of the X-linked mental retardation protein OPHN1 mediates mGluR-dependent LTD through interaction with the endocytic machinery.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

2q23.1 microdeletion identified by array comparative genomic hybridisation: an emerging phenotype with Angelman-like features?

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

The 2q23.1 microdeletion syndrome: clinical and behavioural phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Emerging major synaptic signaling pathways involved in intellectual disability

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Disrupted GABAAR trafficking and synaptic inhibition in a mouse model of Huntington's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Delivery of GABAARs to synapses is mediated by HAP1-KIF5 and disrupted by mutant huntingtin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Impaired alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor trafficking and function by mutant huntingtin.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

A novel microtubule-based motor protein (KIF4) for organelle transports, whose expression is regulated developmentally

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Cell cycle-dependent translocation of PRC1 on the spindle by Kif4 is essential for midzone formation and cytokinesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Human chromokinesin KIF4A functions in chromosome condensation and segregation

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Essential roles of KIF4 and its binding partner PRC1 in organized central spindle midzone formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Evidence for the involvement of KIF4 in the anterograde transport of L1-containing vesicles

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Kinesin family in murine central nervous system

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182

Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defects.

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-102182